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5 months ago
Ametek
Location: Minnesota, United States
Job type: Permanent
Sector: Manufacturing
Category: Office
Job ID #: 9380
Location: US - Minnesota - Montevideo
Functional Area: Engineering
Division: EMG - Engineered Medical Components
Position Type: Full-Time Regular
Department: US - Minnesota - Montevideo
Education Required: Bachelors Degree
Relocation Provided: Some Relocation May Be Available
Experience Required: 3 - 5 Years
Travel Percentage: 25
Hours of Work: 8:00 am - 5:00 pm
Shift: 1st

Position Description

• Identifies new product concepts through familiarity with industry trends, relationships with industry technologists, and collaboration with internal engineering and sales team
• Executes engineering portion of new product introduction (NPI) process and is responsible for the quality of those portions of NPI under active management
• Responsible for successful project execution, reaching milestones, meeting schedules
• Integrates new product design with manufacturing and works closely with development team and manufacturing processes to ensure smooth transition of product concepts to manufacturing (keeps new product development and production process linked)
• Responsible for developing new processes that meet customer product specifications and support EMC's need for reliable and repeatable manufacturing operations
• Responsible to work with development team for product release documentation (risk assessments, validation & test protocols plans, inspection procedures, first article acceptance, production routings, work instructions, and visual aids, etc.)
• Responsible to work with manufacturing team to document the processing steps required to manufacture products, reviews process documentation for accuracy
• Serves as a technical leader of the organization and mentors other engineers
• Provides support to sale teams, interfaces with customer’s principal engineers
* Balances customer expectations and needs with Ametek EMC capabilities and capacity.

Position Requirements

• BS Degree in Engineering or qualifying BS/BA Degree in a related science or discipline
• 5 years engineering experience
• Medical Device/FDA regulatory environment experience is preferred
• Leverages engineering experiences to identify unique design concepts while not being constrained by conventional thinking. Finds relationships between seemingly unrelated issues
• Initiates creative solutions. Ability to develop and implement leading edge technology
• Demonstrated success on innovative programs that require new designs and/or processes
• Broad engineering abilities and understanding of medical interconnect electrical, mechanical, imaging and mfg/industrial engineering disciplines (general understanding of each, with focus in one or more of these disciplines)
• Effective communication, interaction, and cooperation skills with manufacturing, sales, other company personnel, as well as customers and suppliers
• Strong interpersonal skills with the ability to be self managed, give and receive feedback
• Demonstrated success in a team dynamic through leadership, mentoring, and knowledge share
• Ability to effectively manage multiple complex projects of significant financial impact
• Experience with performing DOEs and statistical data analysis highly beneficial
• Proven complex problem solving and decision making abilities
• A working knowledge of SolidWorks, AutoCAD, and/or ProE
• Outgoing personality with a strong desire to provide mentorship
*Experinece in medical device or catheter manufacturing to an ISO13485 standard or similar desired

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

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